OBO ID: DOID:0070197
Term Name: distal myopathy 1 Search Ontology:
Synonyms:
  • Distal myopathy type 1
  • Gowers disease
  • Laing distal myopathy
  • Laing early-onset distal myopathy
  • MPD1
Definition: A distal myopathy that is characterized by autosomal dominant inheritance that has_material_basis_in mutation in the MYH7 gene on chromosome 14q11.2. (2)
References:
Ontology: Human Disease   ( DOID:0070197 )
OTHER distal myopathy 1 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
MYH7 Laing distal myopathy 160500
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None